Method of forming material using atomic layer deposition and method of forming capacitor of semiconductor device using the same
Patent 7425514 Issued on September 16, 2008. Estimated Expiration Date: 
May 10, 2026. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.
May 10, 2026. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.Patent ReferencesMethod for growing thin oxide films Method of film deposition, and fabrication of structures Process for producing aluminum oxide films at low temperatures Conformal thin films over textured capacitor electrodes Method and apparatus for supplying a source gas Patent #: 7007933 InventorsAssigneeApplicationNo. 11430856 filed on 05/10/2006US Classes:438/785, Insulative material is compound of refractory group metal (i.e., titanium (Ti), zirconium (Zr), hafnium (Hf), vanadium (V), niobium (Nb), tantalum (Ta), chromium (Cr), molybdenum (Mo), tungsten (W), or alloy thereof)438/240Having high dielectric constant insulator (e.g., Ta2O5, etc.)ExaminersPrimary: Nguiyen, Tuan H.Attorney, Agent or FirmInternational ClassH01L 21/31DescriptionBACKGROUND OF THE INVENTION1. Field of the Invention The present invention relates to a method of manufacturing semiconductor devices, and more particularly, to a method of forming a material layer during the manufacture of semiconductor devices using the technique of atomic layer deposition (ALD)and a method of forming the dielectric layer of a capacitor of a semiconductor device using ALD. 2. Description of the Related Art The decrease in cell capacitance resulting from a reduction in available memory cell area makes it difficult to increase the integration density of semiconductor memory devices. Decreased cell capacitance degrades the data readability frommemory cells, increases the soft error rate and also hinders low-voltage operation of the semiconductor memory devices. Several techniques have been utilized to maintain or increase the cell capacitance without significantly increasing the wafer area occupied by the memory cell. Two such methods of increasing capacitance within a limited cell area includingthinning the dielectric layer of the capacitor and/or increasing the effective surface area of the capacitor lower electrode using a cylindrical or pin-shaped structure. However, for memory devices such as dynamic random access memories (DRAMs) havingcapacities of 1 gigabit or more, it is difficult to obtain sufficient capacitance to ensure satisfactory operation of the memory devices with either of the methods noted above. To further increase the capacitance that can be achieved within a given memory cell size, research efforts have been directed toward the use of materials having a higher dielectric constant (κ), such as Ta2O.sub.5, Y2O.sub.3,HfO2, ZrO2, Nb2O.sub.5, BaTiO3 or SrTiO3, as the dielectric layer of a capacitor is being actively conducted. Conventionally, a Ta2O.sub.5 film has been widely used because of its relatively high dielectric constant and high thermal stability. However, the use of the Ta2O.sub.5 film has a potential problem in that it typically is highlyreactive with a polysilicon film. If the lower electrode of capacitor is formed from polysilicon, oxygen (O) from the Ta2O.sub.5 film can react with silicon of the polysilicon layer during the formation of the Ta2O.sub.5 film or during asubsequent thermal treatment after the Ta2O.sub.5 film has been formed to from silicon dioxide at the surface of the polysilicon layer. Further, oxygen vacancies within Ta2O.sub.5 film may increase leakage current. In an attempt to address this problem, lower electrodes have been formed from materials that are believed to be relatively more difficult to oxidize than polysilicon. Examples of such materials include noble metals such as platinum (Pt),ruthenium (Ru) and iridium (Ir) or conductive metal nitride films such as titanium nitride (TiN). However, the use of a noble metal or a metal nitride presents other potential problems. A conventional tantalum oxide (Ta2O.sub.5) film is typically formed by chemical vapor deposition (CVD) in an oxygen atmosphere using pentaethoxide tantalum (PET), Ta(OCH3)5 or TaCl5 as a tantalum source gas and oxygen(O2), water (H2O), hydrogen peroxide (H2O.sub.2) or nitrous oxide (N2O) as an oxygen source gas. Notwithstanding any advantages associated therewith, a composition of these source gases often negatively impacts the coverage of theTa2O.sub.5 film, presumably due to the oxidation of the lower electrode. For example, if ruthenium (Ru) is used as a lower electrode, the surface of the Ru layer can be oxidized to form a RuO2 film that minimizes or prevents the formation ofthe desired Ta2O.sub.5 film. This problem often occurs when a Ta2O.sub.5 film is used as a dielectric layer in a cylindrical or concave-shaped capacitor having a large aspect ratio. In such an instance, the Ta2O.sub.5 film will tend tobe more thinly deposited or largely missing from the portion of the Ru electrode in the lower portion of a cylindrical opening, while the Ta2O.sub.5 film is thickly deposited on the upper portion of the opening, thereby resulting in poor stepcoverage of the resulting Ta2O.sub.5 film. Generally, thin films such as dielectric films are formed using deposition methods such as CVD, low-pressure chemical vapor deposition (LPCVD), plasma-enhanced chemical vapor deposition (PECVD) and/or sputtering. The step coverage that istypically obtained with CVD-based methods, however, remained less then desired. Accordingly, atomic layer deposition (ALD) processes have been proposed as an alternative to CVD-based deposition methods because the ALD processes can be performed at lowertemperatures while exhibiting improved step coverage. One such ALD process technology is disclosed in U.S. Pat. No. 6,124,158, in which a first reactant is introduced to react with the treated surface to form a bonded monolayer of reactive species. A second reactant is then introduced to reactwith the bonded monolayer to form a thin layer of the desired material on the treated surface. After each step in the cycle, the reaction chamber is purged with an inert gas to prevent reaction except at the treated surface. Since an ALD film has low thermal budget, excellent step coverage, and excellent thickness control and uniformity, efforts have been made to develop methods whereby a metal oxide such as Ta2O.sub.5, Y2O.sub.3, HfO2, ZrO2, orNb2O.sub.5, may be deposited using an ALD method to form the high-κ dielectric layer of a capacitor. One such effort formed a metal oxide by ALD using as the metal precursor a halide such as HfCl4 in combination with an oxidant such asO2, H2O, H2O.sub.2 or N2O. However, efforts of forming such thin films using halide group precursors tend to result in unsatisfactory levels of step coverage. Further, when H2O is used as the oxidant, hydrogen (H) radicals tend to react with halogen ligands separated from HfCl4 to thereby form a gas including hydrochloric acid (HCl). Because the HCl gas tends to etch the thin film on thesemiconductor device, the surface morphology of the resulting thin film is compromised. In addition, the metal may combine with the --H and/or --OH groups formed, resulting in the incorporation of undesirable impurities, e.g., metal hydroxides, into themetal oxide film. If a metal oxide film containing impurities such as metal hydroxides is utilized as a dielectric layer in a semiconductor device, the metal hydroxides may act as trap sites or a current leakage sites, thereby degrading the dielectriccharacteristics of the resulting device. SUMMARY OF THE INVENTION In an exemplary embodiment, the present invention provides a method of forming a material using atomic layer deposition (ALD) having improved step coverage and leakage current preventing characteristics. In an exemplary embodiment, the present invention provides a method of forming a semiconductor capacitor having a large aspect ratio in which oxidization of the lower electrode is suppressed in order to form a metal oxide thin film havingimproved uniformity In an exemplary embodiment, the present invention provides a method of forming a material utilizing an ALD process comprising the steps of: (a) introducing a first reactant containing a first atom necessary to form the material and at least onealkoxide group on a substrate; (b) chemisorbing a portion of the first reactant onto the substrate; (c) introducing a second reactant that is activated and does not contain a hydroxyl group to the substrate; and (d) chemically reacting the secondreactant with the chemisorbed first reactant to form an atomic layer of the material on the substrate. In an exemplary embodiment, the atomic layer formed on the substrate can serve as a dielectric layer of a capacitor for a semiconductor device or as a gate dielectric layer for a semiconductor device. In an exemplary embodiment, the present invention provides a method of forming a thin film using an ALD process comprising the steps of: (a) placing a substrate into a chamber; (b) introducing a first reactant including a metal alkoxide into thechamber; (c) chemisorbing a portion of the first reactant onto the substrate; (d) removing non-chemically adsorbed first reactant from the chamber; (e) introducing a second reactant as an activated oxidant that lacks a hydroxyl group into the chamber;(f) chemically reacting the second reactant with the chemisorbed first reactant to form an atomic layer of a metal oxide film on the substrate; and (g) removing the non-chemically reacted second reactant from the chamber. In an exemplary embodiment, the present invention provides a method of forming a capacitor comprising the steps of: (a) forming a first electrode on a semiconductor substrate; (b) introducing a first reactant containing a first atom for forming adielectric material and at least one alkoxide group on the first electrode; (c) chemisorbing a portion of the first reactant onto the first electrode; (d) introducing a second reactant containing no hydroxyl group on the first electrode; (e) chemicallyreacting the second reactant with the chemisorbed first reactant to form a dielectric layer on the first electrode; and (f) forming a second electrode on the dielectric layer. According to an exemplary embodiment, the present invention involves an ALD process in which a metal alkoxide precursor and an oxidant that contains no hydroxyl group may be reacted to form a thin film having improved step coverage and animproved leakage current characteristics. When such a thin film is used as the capacitor dielectric layer or as the gate dielectric layer in a semiconductor device, the reliability of the resulting semiconductor device may also be improved. BRIEF DESCRIPTION OF THE DRAWINGS Exemplary embodiments of the present invention will become apparent by reference to the following detailed description when considered in conjunction with the accompanying drawings wherein: FIGS. 1A to 1E are cross-sectional views illustrating a method of forming a material using atomic layer deposition according to an exemplary embodiment of the present invention; FIG. 2 is a graph showing a deposition rate of hafnium oxide (HfO2) film versus the deposition temperature in accordance with an exemplary embodiment of the present invention; FIG. 3 is a graph showing a thickness of HfO2 film versus the deposition cycle in accordance with an exemplary embodiment of the present invention; FIGS. 4A and 4B are graphs showing the binding status of HfO2 film as a function of post annealing and deposition temperature respectively in accordance with an exemplary embodiment of the present invention; FIG. 5 is a graph showing a depth profile of a HfO2 film formed according to an exemplary embodiment of the present invention; FIGS. 6A to 6E are cross-sectional views illustrating a method of manufacturing a semiconductor device in accordance with an exemplary embodiment of the present invention; FIG. 7 is a graph showing the leakage current of a capacitor manufactured according to an exemplary embodiment of the present invention; FIG. 8 is a cross-sectional view of a cylinder type capacitor in accordance with an exemplary embodiment of the present invention; FIGS. 9A and 9B are schematic views showing a cross-section of a substrate photographed by scanning electron microscope (SEM), in case that a Ta2O.sub.5 films are formed using H2O and O2 as an oxygen source, respectively inaccordance with an exemplary embodiment of the present invention; FIG. 10 is a graph showing equilibrium vapor pressures of PET and TAT-DMAE precursors versus temperature in accordance with an exemplary embodiment of the present invention; and FIG. 11 is a cross-sectional view schematically illustrating an adsorption mechanism of gaseous tantalum precursors on a Ru lower electrode in accordance with an exemplary embodiment of the present invention. DESCRIPTION OF EXEMPLARY EMBODIMENTS Hereinafter, the preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. In the following drawings, the same numerals are used to indicate the same or corresponding elements. FIGS. 1A to 1E are cross-sectional views illustrating a method of forming a material using atomic layer deposition according to an exemplary embodiment of the present invention. Referring to FIG. 1A, a substrate 1 including a semiconductor material such as silicon (Si) is placed into a deposition chamber (not shown). A first reactant 2 containing a first atom (e.g., a metal or a semimetal) necessary to produce thedesired material and at least one alkoxide group as a ligand is then introduced into the chamber. In an exemplary embodiment, the first reactant 2 is a metal alkoxide. The metal alkoxide may include a second group metal alkoxide including at least onesecond group metal such as magnesium (Mg), calcium (Ca) or strontium (Sr), a third group metal alkoxide including at least one third group metal such as boron (B), aluminum (Al) or lanthanum (La) (even though boron is considered a semimetal), a fourthgroup metal alkoxide including at least one fourth group metal such as titanium (Ti), zirconium (Zr), hafnium (Hf), silicon (Si), germanium (Ge), tin (Sn) or lead (Pb) (even though silicon and germanium are more commonly considered semimetals) and afifth group metal alkoxide including at least one fifth group metal such as vanadium (V), niobium (Nb), tantalum (Ta), phosphorus (P), arsenic (As) or antimony (Sb) (even though P is not generally considered a metal and As and Sb are more commonlyconsidered semimetals). In an exemplary embodiment of the present invention, the metal alkoxide is a fourth group metal alkoxide. An example of a Mg alkoxide is Mg[OC2H.sub.4OCH.sub.3]2, an example of a Ca alkoxide is Ca[OC2H.sub.4OCH.sub.3]2, and an example of a Sr alkoxide is Sr[OC2H.sub.4OCH.sub.3]2. Examples of B alkoxides includeB[OCH3]3, B[OC2H.sub.5]3, B[OC3H.sub.7]3 and B[OC4H.sub.9]3, examples of Al alkoxides include Al[OC2H.sub.4OCH.sub.3]2, Al[OCH3]3, Al[OC2H.sub.5]3, Al[OC3H.sub.7]3 andAl[OC4H.sub.9]3, and examples of La alkoxides include La[OC2H.sub.4OCH.sub.3]2 and La[OC3H.sub.7CH.sub.2OC.sub.3H.sub.7]3. Examples of Ti alkoxides include Ti[OCH3]4, Ti[OC3H.sub.7]4, Ti[OC4H.sub.9]4 and Ti[OC2H.sub.5]2[OC2H.sub.4N(CH3)2]2, examples of Zr alkoxides include Zr[OC3H.sub.7]4,Zr[OC4H.sub.9]4 and Zr[OC4H.sub.8OCH.sub.3]4, examples of Hf alkoxides include Hf[OC4H.sub.9]4, Hf[OC4H.sub.8OCH.sub.3]4, Hf[OC4H.sub.9]2[OC2H.sub.4N(CH3)2]2,Hf[OC4H.sub.9]2[OC4H.sub.8OCH.sub.3]2, Hf[OSi(C2H.sub.5)3]4, Hf[OC2H.sub.5]4, Hf[OC3H.sub.7]4, Hf[OC4H.sub.9]4 and Hf[OC5H.sub.11]4. Examples of Si alkoxides includeSi[OCH3]4, Si[OC2H.sub.5]4, Si[OC3H.sub.7]4, HSi[OCH3]3, HSi[OC2H.sub.5]3, Si[OCH3]3F, Si[OC2H.sub.5]3F, Si[OC3H.sub.7]3F and Si[OC4H.sub.9]3F, examples of Gealkoxides include Ge[OCH3]4, Ge[OC2H.sub.5]4, Ge[OC3H.sub.7]4 and Ge[OC4H.sub.9]4, examples of an Sn alkoxide include Sn[OC4H.sub.9]4 and Sn[OC3H.sub.7]3[C4H.sub.9], and examples of Pbalkoxides include Pb[OC4H.sub.9]4 and Pb4O[OC4H.sub.9]4. Examples of V alkoxides include VO[OC2H.sub.5]3 and VO[OC3H.sub.7]3, examples of Nb alkoxides include Nb[OCH3]5, Nb[OC2H.sub.5]5, Nb[OC3H.sub.7]5 and Nb[OC4H.sub.9]5, examples of Taalkoxides include Ta[OCH3]5, Ta[OC2H.sub.5]5, Ta[OC3H.sub.7]5, Ta[OC4H.sub.9]5, Ta[OC2H.sub.5]4[OC2H.sub.4N(CH3)2] and Ta[OC2H.sub.5]4[CH3COCHCOCH.sub.3], examples of Palkoxides include P[OCH3]3, P[OC2H.sub.5]3, P[OC3H.sub.7]3, P[OC4H.sub.9]3, PO[OC2H.sub.5]3, PO[OC3H.sub.7]3 and PO[OC4H.sub.9]3, examples of As alkoxides include As[OCH3]3,As[OC2H.sub.5]3, As[OC3H.sub.7]3 and As[OC4H.sub.9]3, and examples of Sb alkoxides include Sb[OC2H.sub.5]3, Sb[OC3H.sub.7]3 and Sb[OC4H.sub.9]3. Referring to FIG. 1B, during the step of introducing the first reactant 2, a first portion of the first reactant 2 chemisorbs and forms a layer 4 on the surface of the substrate 1. A second portion of the first reactant 2 is physically attached(physisorbed) onto and is loosely held to the chemisorbed layer 4 of the first reactant 2. The chamber may then be purged with an inert gas such as argon (Ar) or nitrogen (N2), and vacuum purged to remove the non-chemically absorbed portions of thefirst reactant 2 from the chamber, leaving the chemisorbed layer 4 of the first reactant 2 intact on the substrate 1. Referring to FIG. 1C, a second reactant 6 comprising an activated oxidant that does not contain a hydroxyl group is introduced into the chamber to chemically react the second reactant 6 with the chemisorbed first reactant 2, and thereby form anatomic layer 8 of the desired material on the substrate 1. The non-chemically reacted portion of the second reactant is then removed from the chamber. That is, the first atom (metal or non-metal) from the chemisorbed first reactant 2 reacts with oxygenof the second reactant 6 to form a metal oxide film as the unit of atomic layer. The second reactant 6 is an activated oxidant that can form oxygen (O) radicals and may be ozone (O3), plasma O2, remote plasma O2 or plasma N2O. Whenan oxygen gas is treated with an O3 generator, a portion of O2 gas is converted into O3, thereby producing a mixed gas comprising O2 and O3 with the O3 gas typically present in a mole percent of about 5 to 15%. Referring to FIG. 1D, the chamber is then purged with an inert gas such as Ar or N2, and then vacuum purged, to remove the non-chemically reacted portions of the second reactant 6 from the chamber. The steps of introducing the first reactant, purging the first reactant, introducing the second reactant and purging the second reactant can be repeated to achieve any desired thickness of material layer 8a. The material layer 8a is aninsulating layer, and may be a metal oxide layer including a metal oxide such as HfO2, ZrO2, Ta2O.sub.5, Y2O.sub.3, Nb2O.sub.5, TiO2, CeO2, In2O.sub.3, RuO2, MgO, Sro, B2O.sub.3, SiO2, GeO2,SnO2, PbO, PbO2, V2O.sub.3, La2O.sub.3, As2O.sub.5, As2O.sub.3, Pr2O.sub.3, Sb2O.sub.3, Sb2O.sub.5, CaO or P2O.sub.5. Since metal alkoxides known as precursors for CVD processes tend to decompose at a higher temperatures, ALD processes using the metal alkoxide may be carried out at a temperature of between about 100 and 500° C., and may typically becarried out at a temperature of less than about 400° C. Metal alkoxides tend to have higher vapor pressures than that of other precursors, e.g., halide precursors under similar process conditions. A higher vapor pressure indicates that there area relatively larger number of gas molecules when compared to a system having a lower vapor pressure. With respect to the metal alkoxides, the amount of metal source gas provided to the deposition chamber is relatively large, thus increasing the relativenumber of molecules made available for reaction at the bottom of the stepped region. Therefore, the metal alkoxide and other alkoxides employed as precursors in accordance with the exemplary embodiments of the present invention can form a thin filmexhibiting improved step coverage when compared with conventional precursors. In an exemplary embodiment, a thin film is formed using an ALD method using precursors of an alkoxide group, e.g., a tetra-butoxy-hafnium [Hf(OtBu)4], and oxygen (O2) gas may be formed with a lower thermal budget than a conventionalCVD-HfO2 film that would typically be deposited at a higher temperature of about 500° C. or more, thereby causing a higher thermal budget. Further, the ALD-HfO2 film thickness may be controlled to a thickness of 20 Å or less, incomparison with the CVD-HfO2 film that will typically be deposited to a thickness of at least several tens of Angstroms. Ozone (O3) gas used as an activated oxidant can oxidize a metal while generating no, or substantially no, by-products when compared with conventional oxidants. According to exemplary embodiments of the present invention, a second reactantthat does not contain a hydroxyl group may be utilized to suppress the formation of undesirable impurities such as a metal-OH bond, thereby producing a thin film having improved stoichiometry and dielectric properties. Hereinafter, a method of forming a HfO2 film to act as the capacitor dielectric layer or gate dielectric layer using ALD process in accordance with an exemplary embodiment of the present invention will be described. A substrate such as a silicon wafer is placed in a chamber that maintains a temperature of about 300° C. and the chamber is evacuated to a pressure of about 0.4 Torr. Using an inert carrier gas such as argon (Ar) or nitrogen (N2), aflow of 200 sccm of a first reactant containing a first atom necessary for forming the desired dielectric film, i.e., hafnium, and an alkoxide group may be introduced into the chamber (on the substrate) for about 1 second. Although as the firstreactant, one or more hafnium alkoxides such as Hf(OEt)4, Hf(OPr)3, Hf(OBu)4[Hf(OnBu)4, Hf(OtBu)4], Hf(mmp)4, Hf(OtBu)2(dmae)2, Hf(OtBu)2(mmp)2 or Hf[OSi(C2H.sub.5)4 may be used, Hf(OtBu)4was utilized in the exemplary embodiment described further below. In the shorthand notation used above, "Et" denotes an ethyl group, "Pr" denotes a prophyl group, "nBu" denotes an n-butyl group, "tBu" denotes a t-butyl group, "dmae" denotes a dimethyaminoethoxide group (--OC2H.sub.4N(CH3)2) and"mmp" denotes a 1-methoxy-2-methyl-2-propoxy group (--OC4H.sub.8OCH.sub.3). During the introduction of the first reactant, a first portion of the Hf(OtBu)4 chemisorbs and forms a layer on the surface of the substrate. A second portion of Hf(OtBu)4 physically attaches (physisorbs) onto and is loosely held tothe chemisorbed layer of Hf(OtBu)4. Hf(OtBu)4 is a liquid at a room temperature, may be represented by Formula I as illustrated below, and has a vapor pressure of 0.5 Torr at a temperature of 50.3° C. ##STR00001## The chamber (substantially, the upper portion of the substrate) is purged with an inert gas such as Ar or N2 and vacuum purged. During the purging steps, the non-chemically absorbed portions of Hf(OtBu)4 are removed from the chamberwhile the chemisorbed layer of Hf(OtBu)4 remains intact on the substrate. A flow of 200 sccm of a second reactant comprising an activated oxidant containing no hydroxyl group, such as O3, plasma O2, remote plasma O2 or plasma N2O, is then introduced into the chamber for about 2 seconds. This allowsan activated oxygen (O) from the second reactant to react with the chemisorbed Hf(OtBu)4 on the substrate to form a HfO2 film as an atomic layer on the substrate. The chamber is then purged with an inert gas such as Ar or N2 and then, vacuum purged to remove substantially all of the non-chemically reacted second reactant from the chamber. The steps of introducing Hf(OtBu)4 into the chamber,purging the chamber, introducing the activated oxidant into the chamber and purging the chamber can be repeated as necessary to achieve any desired thickness of the resulting HfO2 film. During these steps, in an exemplary embodiment, thetemperature of the chamber is maintained at a temperature below about 400° C., such as a temperature of about 300° C. According to exemplary embodiments of the present invention, hafnium alkoxide precursors such as Hf(OtBu)4, which have a higher vapor pressure than other precursors such as hafnium halides such as HfCl4, may be used to form a HfO2film with improved step coverage. Further, by using an activated oxidant that contains no hydroxyl group the formation of impurities in which a hafnium (Hf) bonds with --H or --OH may be suppressed or eliminated, thereby obtaining a HfO2 filmhaving improved stoichiometry that contains few or no impurities that could act as electron trap sites or current leakage sites. After depositing the HfO2 film with an ALD process using Hf(OtBu)4 and O3 as described above, various characteristics of the HfO2 film were observed through the following experiments. In exemplary embodiments, the dosingstep, Ar purging step, O3 dosing step and Ar purging step were carried out for one second, two seconds, two seconds and two seconds, respectively. The ALD process was also performed at various exemplary deposition temperatures including 250° C., 300° C., 350° C. and 400° C. FIG. 2 is a graph showing a deposition rate of HfO2 film versus the deposition temperature. In the graph, the horizontal axis represents the deposition temperature (° C.) and the vertical axis represents the deposition rate(Å/cycle). As reflected in FIG. 2, the deposition rate of HfO2 film was at a minimum at the deposition temperature of about 300° C. and increased at a temperature of about 400° C. Accordingly, the HfO2 film exhibitsstronger ALD characteristics when deposited at a temperature of in the vicinity of 300° C., while the properties of the film deposited at 400° C. or more begins to resemble those of a CVD-deposited film. Therefore, in an exemplaryembodiment the HfO2 film is deposited at a temperature of 400° C. or less, and in another exemplary embodiment, 250 to 350° C. FIG. 3 is a graph showing a thickness of HfO2 film versus the deposition cycle. In the graph, the horizontal axis represents the deposition cycle and the vertical axis represents the film thickness. The deposition process was performed ata temperature of 300° C. Referring to FIG. 3, since the HfO2 film has ALD characteristics in the vicinity of 300° C., the thickness of HfO2 film linearly increased in accordance with the deposition cycle. Accordingly, the HfO2 film deposited by anALD process using Hf(OtBu)4 and O3 exhibits improved thickness control and uniformity, thereby decreasing pattern loading effects. Further, for HfO2 films deposited by an ALD process using Hf(OtBu)4 and O3, exhibited stepcoverage (the thickness ratio of the film formed on the upper portion of the structure to film formed on the lower portion of the structure) of about 80% or more on a structure having an aspect ratio of more than about 13:1. FIG. 4A is a graph showing the binding status of oxygen examined through an X-ray photoelectric spectroscopy (XPS) analysis of as-deposited and post-annealed HfO2 film. In FIG. 4A, a trace (a) indicates the binding status of as-depositedHfO2 film, and a trace (b) indicates the binding status of post-annealed HfO2 film. In the graph, the horizontal axis represents a binding energy (eV) and the vertical axis represents intensity. Referring to FIG. 4A, a number of C--O bonds was detected in the as-deposited HfO2 film. However, the C--O bonds within HfO2 film nearly vanished and the Hf--O binding energy was shifted in the opposite direction of Hf metal phaseafter post-annealing. Accordingly, the binding status within the HfOx film was stabilized by the post-annealing. FIG. 4B is a graph showing the binding status of Hf examined through an XPS analysis of post-annealed HfO2 film after the deposition of HfO2 film was carried out at various temperatures. In FIG. 4B, the horizontal axis represents abinding energy (eV) and the vertical axis represents intensity. As reflected in FIG. 4B, the binding status of HfO2 film appeared to be most stable for films formed at the deposition temperature of about 350° C. FIG. 5 is a graph showing a depth profile of HfO2 film in accordance with an exemplary embodiment of the present invention. The depth profile was observed by a time of flight-secondary ion-mass spectrometer (TOF-SIMS). In the graph, thehorizontal axis represents time (seconds) and the vertical axis represents intensity. As reflected in FIG. 5, Hf--O bonds were uniformly detected in the HfO2 film through the substantially full thickness of the HfO2 film, confirming theformation of a generally uniform HfO2 film that contains no significantly impurities such as Hf(OH)2 that could act as electron trap sites or current leakage sites. Exemplary Method of Manufacturing a Semiconductor Device FIGS. 6A to 6E are cross-sectional views illustrating a method of manufacturing a semiconductor device in accordance with an exemplary embodiment of the present invention. Referring to FIG. 6A, a semiconductor substrate 100 is divided into anactive region 101 and an isolation region (or field region) 102 on which are formed transistors including a gate dielectric layer 104, a gate electrode 110, and source/drain regions 116a and 116b. Since a very thin gate dielectric layer of about 10Å is needed in a semiconductor memory device having a capacity of 1 gigabit or more, the gate dielectric layer 104 may be formed using an exemplary embodiment of the present invention. Specifically, as shown in FIGS. 1A to 1E, an ALD process usingmetal alkoxide precursors and an activated oxidant such as O3, plasma O2, remote plasma O2 or plasma N2O, may be utilized to form the gate dielectric layer 104 from a metal oxide film. In an exemplary embodiment, the gate dielectriclayer 104 of HfO2 is formed by an ALD process using Hf(OtBu)4 and O3. In an exemplary embodiment, the gate electrode 110 may have a polycide structure including an impurity-doped polysilicon layer and a metal silicide layer stacked thereon. A capping insulating layer 112 and sidewall spacers 114 are formed on thetop and side of the gate electrode 110, respectively. In an exemplary embodiment, the capping insulating layer 112 and sidewall spacers 114 may be formed from a silicon oxide, a silicon nitride or other suitable insulating material. Referring to FIG. 6B, a first insulating layer 118 comprising an oxide is formed on the entire surface of the substrate 100 on which the transistors are formed. Then, a portion of the first insulating layer 118 is etched away through aphotolithography process to thereby form a contact hole 120 to partially expose the source region 116a. A first conductive layer, e.g., a P-doped polysilicon layer, is deposited on the contact hole 120 and the first insulating layer 118. Through an etch-back process or chemical-mechanical polishing (CMP) process, the first conductive layer isremoved until the surface of the first insulating layer 118 is exposed, thereby forming a contact plug 122 in the contact hole 120. Referring to FIG. 6C, an etch stopping layer 123 is formed on the contact plug 122 and the first insulating layer 118. The etch stop layer 123 comprises a material having a high etch selectivity with respect to the first insulating layer 118,for example, silicon nitride (SixN.sub.y) or silicon oxynitride (SiON) (that is, the etch rate of the first insulating layer 118 is much higher than the etch rate of the etch stopping layer 123 under similar etch conditions). After forming a second insulating layer 124 comprising an oxide on the etch stop layer 123, a portion of the second insulating layer 124 and a portion of the etch stop layer 123 are etched away to form an opening 126 that exposes a surface of thecontact plug 122. Specifically, after etching the second insulating layer 124 until the etch stopping layer 123 is exposed, an over-etching process is carried out for a desired time to complete opening 126 and expose a surface of the contact plug 122and an adjacent portion of the first insulating layer 118. The opening 126 may be formed with a non-vertical sidewall slope such that the inlet of the opening 126 is wider than the bottom thereof. This is because the etch rate of the bottom of theopening 126 is decreased relative to the etch rate at the inlet of the opening 126 due to loading effects during the etching process. A second conductive layer 127 is deposited on the side and bottom of the opening 126 and the top of the second insulating layer 124. In an exemplary embodiment, the second conductive layer 127 may comprise a semiconductor material such aspolysilicon, noble metals such as Ru, Pt, Ir or a combination thereof, or a conductive metal nitride such as TiN, TaN, WN or a combination thereof. Referring to FIG. 6D, after forming a sacrificial layer (not shown) on the second conductive layer 127 and the opening 126, the upper portion of the sacrificial layer is etched back or otherwise removed such that the only remaining portion of thesecond conductive layer 127 is found on the side and bottom of the opening 126. By doing so, the second conductive layer 127 deposited on the surface of the second insulating layer 124 is removed to separate the second conductive layer 127 depositedalong the profile of the opening 126 into a cell unit. The sacrificial layer is then removed to form a lower electrode 128 of a capacitor on each of the memory cell regions. The lower electrode 128 has a generally tapered cylindrical shape wherein theinlet is wider than the bottom and a height of about 10,000 to 17,000 Å. Upon the lower electrode 128, as shown in FIGS. 1A to 1E, a layer of HfO2 may then be deposited by an ALD process using hafnium alkoxide precursors such as Hf(OtBu)4 and an activated oxidant such as O3, plasma O2, remoteplasma O2 or plasma N2O, to form dielectric layer 130 of the capacitor. As described above, an ALD process using hafnium alkoxide precursors and an activated oxidant is utilized to obtain the dielectric layer 130 having an excellent stepcoverage in which the ratio of an upper thickness (t1) to a lower thickness (t2) is no less than 1:0.8 on a lower electrode 128 having an aspect ratio of 13:1 or more. The dielectric layer 130 may be formed from a single layer of HfO2 or may be acomposite layer of two or more metal oxides deposited sequentially. For example, Hf and Al metal precursors utilized in the exemplary ALD process may be alternated to form a dielectric layer 130 having a stacked structure consisting of alternatingAl2O.sub.3 and HfO2 layers. The number and relative thickness of the layers in such heterogeneous dielectric layers may be adapted as desired to obtain a variety of dielectric films. If the lower electrode 128 is formed from polysilicon, oxygen (O) separated from the oxidant may react with the silicon of the lower electrode 128 during the formation of the dielectric layer 130, thereby resulting in some oxidation of the lowerelectrode 128. Accordingly, before forming the dielectric layer 130 on a polysilicon electrode, a rapid thermal nitridation may be carried out in an atmosphere containing N2 gas or ammonia to nitrify the surface of the lower electrode 128, therebypreventing or reducing the reaction of the oxidant used to form the dielectric layer 130 with the lower electrode 128. Referring to FIG. 6D, after completing the formation of the dielectric layer 130 by the ALD process using metal alkoxide precursors and an ozone oxidant, the dielectric layer 130 may be annealed in an oxidizing atmosphere such as UV-O3, toreduce or eliminate contaminants and cure oxygen defects. An upper electrode 132 of the capacitor is deposited on the dielectric layer 130 to form the capacitor (C) including the lower electrode 128, the dielectric layer 130 and the upper electrode 132. The upper electrode 130 may comprise asemiconductor material such as polysilicon, noble metals including Ru, Pt, Ir or a combination thereof, or a conductive metal nitride including TiN, TaN, WN or a combination thereof. In an exemplary embodiment, the upper electrode 132 is formed as astacked structure of TiN/polysilicon. FIG. 7 is a graph showing a leakage current of the capacitor having a dielectric layer formed by the ALD process in accordance with an exemplary embodiment of the present invention. In the graph, the horizontal axis represents an applied voltage(V) and the vertical axis represents the measured leakage current (A/cell). The capacitor was formed through the method shown in FIGS. 6A to 6E. Specifically, the surface of the lower electrode consisting of P-doped polysilicon was nitrified by rapid thermal process (RTP) using NH3 gas. An exemplary ALD processusing Hf(OtBu)4 and O3 was then used to form a first HfO2 film to a thickness of about 20 Å that was annealed using UV-O3. A second ALD HfO2 film of about 50 Å was then deposited on the first ALD HfO2 film usingHf(OtBu)4 and O3, followed by a second anneal using UV-O3 to produce a HfO2 film consisting of two atomic layers. A TiN film was then deposited on the HfO2 film using TiCl4 and NH3 source gases and a P-dopedpolysilicon film was, in turn, deposited on the TiN film to form an upper electrode consisting having a TiN/polysilicon stacked structure. As shown in FIG. 7, the capacitor manufactured according to exemplary embodiments of the present invention exhibits a leakage current of less than 1 fA/cell at 1V. Accordingly, capacitors utilizing a HfO2 dielectric layer manufactured inaccord with the exemplary embodiments of the present invention exhibits improved electric characteristics including a more stable leakage current, even when deposited on a electrode structure having an aspect ratio of 13:1 or more. Second Exemplary Method of Manufacturing a Semiconductor Device FIG. 8 is a cross-sectional view of a cylindrical capacitor in accordance with another exemplary embodiment of the present invention. Although as described in connection with this exemplary embodiment, the capacitor is cylindrical, it should beappreciated that the capacitor electrodes may be formed in a wide range of geometries. Referring to FIG. 8, the cylindrical capacitor has a structure in which a TEOS layer 200 is patterned and etched to form a cylindrical shape on a semiconductor substrate (not shown). A lower electrode 210, a Ta2O.sub.5 dielectric layer 220and an upper electrode 230, which then sequentially stacked along the TEOS layer 200. The lower electrode 210 and the upper electrode 230 may be comprise polysilicon, a noble metal such as Ru, Pt, Ir or a combination thereof, or a conductive metalnitride such as TiN, TaN, WN or a combination thereof. In addition to embodiments utilizing a single metal nitride layer, a solid solution nitride layer such as (Ti, Ta)N can be used as the upper electrode, along with other materials. Similarly, acomposite electrode formed by depositing or otherwise forming layers of at least two of the noted conductive materials described above can be used. In exemplary embodiments of the present invention, the Ta2O.sub.5 layer is deposited using tantalum precursors of a monomer expressed by Formula II and ozone gas as source gases. ##STR00002## As shown in Formula II, X has a coordinate bond with Ta formed through an unshared electron pair. In an exemplary embodiment, X may be N, S, O, or C=O and R1 and R2 may be independently selected alkyl groups such as a C1 toC4 alkyl group. In an exemplary embodiment, R1 and R2 are methyl groups. In an exemplary embodiment, ozone gas is used as an oxygen source for depositing the Ta2O.sub.5 layer. The O3 gas can be used as an oxidizer for forming a Ta2O.sub.5 layer at a temperature below 400° C., in contrast to thethermal conditions employed using O2, H2O or N2O. It should be appreciated that other temperature conditions can be employed. The Ta2O.sub.5 layer can be formed by thermal chemical vapor deposition (CVD) or atomic layer deposition (ALD) techniques, as well as other techniques. According to the thermal CVD method, tantalum precursors and ozone gas simultaneouslyflow into a deposition chamber. Conversely, tantalum precursors and ozone gas sequentially flow into a deposition chamber to deposit a Ta2O.sub.5 layer using an ALD method. One example of an ALD method of forming a Ta2O.sub.5 layer in accordance with exemplary embodiments the present invention may be carried out as follows. It should be appreciated that variations from this method can occur with departing fromthe scope of the invention. A semiconductor substrate on which a lower electrode 210 is formed is introduced into a deposition chamber. A flow of 1-2000 sccm of a first reactant including a first atom, i.e., tantalum (Ta), for forming the desired thin film and at least onealkoxide group, i.e., tantalum precursors expressed by Formula II, is introduced into the chamber so that the first reactant is chemically or physically absorbed on the surface of an Ru electrode 210 of the semiconductor substrate. The tantalumprecursors are typically provided by a bubbling method or a liquid delivery system (LDS) method. After the adsorption is completed and a desired time has elapsed, a flow of 1-2000 sccm of an inert purge gas such as argon or nitrogen is introduced into the chamber to remove the remaining tantalum precursors from the chamber, while theadsorbed tantalum precursors remain in the chamber. After the purge is completed, the inflow of the purge gas is stopped and a flow of 1-2000 sccm of a second reactant, i.e., ozone gas, is introduced into the chamber. The ozone gas then reacts with the adsorbed tantalum precursors to form aTa2O.sub.5 layer. After the inside of the deposition chamber is again purged with an inert gas such as argon or nitrogen, a cycle of: (1) inflow of tantalum precursors, (2) inflow of purge gas, (3) inflow of ozone gas, and (4) inflow of purge gasmay be carried out repeatedly to form a Ta2O.sub.5 layer 220 having a desired thickness. During the deposition, the temperature of the chamber may range from about 100° C. to about 600° C., and the pressure of the chamber may range from about 0.1 Torr to about 30 Torr. After the formation of the lower electrode 210 and before the formation of the Ta2O.sub.5 layer 220, a process for forming a tantalum preprocessed layer (not shown) can be additionally performed by repeating the inflow and purging of thetantalum precursors expressed by Formula II. This sequence can result in the simplification of the formation of the Ta2O.sub.5 layer. In such an exemplary embodiment, a thin Ta2O.sub.5 layer is formed on the lower electrode with the tantalumprecursors. Due to the presence of the Ta2O.sub.5 layer, the oxidation of the lower electrode in an oxygen atmosphere may be reduced or prevented. Thus, a Ta2O.sub.5 layer having superior step coverage may be obtained. An upper electrode 230 is formed on the dielectric layer 220, the dielectric layer 220 being fabricated as set fourth above. The upper electrode 230 can comprise polysilicon, a noble metal such as Ru, Pt, Ir or a combination thereof, or aconductive metal nitride such as TiN, TaN, WN or a combination thereof. In addition to an employment of a single metal nitride layer, a solid solution nitride layer such as (Ti, Ta)N can be used as the upper electrode, along with other materials. Also,a composite layer formed by depositing at least two of the conductive materials described above can be used. Experiment 1 A tantalum dielectric layer was formed on a cylindrical Ru lower electrode having an aspect ratio of about 15:1 using tetraethoxy tantalum dimethylamino-ethoxide (TAT-DMAE) as a tantalum precursor and O3 gas as an oxygen source. Thedielectric layer was formed by an ALD method having a cycle of inflow of tantalum precursors->purging->inflow of O3 gas->purging. In this experiment, the temperature of the chamber was maintained at temperatures of 250° C.,300° C., 350° C. and 400° C. The thickness of the upper portion of a Ta2O.sub.5 layer deposited at each temperature (t1 of FIG. 8) and the thickness of the lower portion of the Ta2O.sub.5 layer (t2 of FIG. 8)were measured. The results of these measurements are shown below in Table 1. TABLE-US-00001 TABLE 1 Classification 250° C. 300° C. 350° C. 400° C. t1 (Å) 240 103 233 244 t2 (Å) 220 102 207 228 As shown in Table 1, the thicknesses of the deposited layers vary with temperature. Notwithstanding these differences, it was observed that the Ta2O.sub.5 layer exhibited thickness uniformity of at least about 90% with respect to the layerformed on upper portions and lower portions. Comparative Example 1 For comparison with the present invention, a Ta2O.sub.5 layer was formed by ALD method at a temperature of 350° C. using PET as the tantalum precursor and O2 and H2O gases as the oxygen sources, respectively. FIGS. 9A and 9B schematically illustrates sections of the substrate when Ta2O.sub.5 layers are formed using the above-mentioned oxygen sources. When H2O was employed as the oxygen source gas, the Ta2O.sub.5 layer 220 was deposited on the upper portion of the opening 240, but the Ta2O.sub.5 layer 220 was not deposited on the lower portion of the opening 240. It is believedthat the formation of the Ta2O.sub.5 layer 220 was prevented due to the presence of RuO2 210' formed by surface oxidation of the Ru layer 210 under the opening 240. As shown in FIG. 9B, when O2 is employed as the oxygen source gas, no Ta2O.sub.5 layer was deposited on the entire surface of the opening 240. Comparative Example 2 Ta2O.sub.5 layers were formed by ALD method at temperatures of 250° C., 300° C., 350° C. and 400° C. using PET as tantalum precursor and O3 as an oxygen source. This example illustrates similar results to Comparative Example 1 that employed H2O as the oxygen source gas. Referring to FIG. 9A, the Ta2O.sub.5 layer 220 was deposited on the upper portion of the cylindrical opening 240 at eachtemperature, but the Ta2O.sub.5 layer was not deposited on the lower portion of the opening 240. Further, as the deposition temperature was increased, the depth to which the Ta2O.sub.5 layer 220 was formed (designated as h in FIG. 9A) tendedto increase. Table 2 illustrates the thicknesses (designated as t1 and t2 in FIG. 8) of the upper portion and lower portion of the Ta2O.sub.5 layer 220 formed at 300° C. and 350° C., and also the depth to which theTa2O.sub.5 layer 220 was formed (designated as h in FIG. 9A). TABLE-US-00002 TABLE 2 Classification 300° C. 350° C. t1 (Å) 549 456 t2 (Å) ~0 ~0 H (Å) 3300 6700 Although not intending to be bound by theory, one possible reason as to why tantalum precursors of exemplary embodiments of the present invention expressed by Formula II display superior coverage to other tantalum precursors such as PET will bedescribed with respect to steric hindrance believed to be attributable to equilibrium vapor pressure and sticking probability impacting the tantalum precursor molecular structure. FIG. 10 illustrates equilibrium vapor pressure with respect to temperatures of PET and TAT-DMAE. As reflected in FIG. 10, the equilibrium vapor pressure of TAT-DMAE is higher than that of PET. Therefore, at the same temperature, the equilibriumvapor pressure of TAT-DMAE is generally higher than that of PET over a given temperature range. In accordance with exemplary embodiments of the present invention, since a tantalum precursor source gas is provided at 140° C. with respect to PETand at 120° C. with respect to TAT-DMAE, the equilibrium vapor pressure of TAT-DMAE is observed to be about twice as great as that of PET. A high equilibrium vapor pressure indicates that there are a greater number of gas molecules relative to asystem having a lower equilibrium vapor pressure. With respect to a TAT-DMAE system, the amount of tantalum source gas provided into the deposition chamber is sizeable. Accordingly, the number of molecules directly provided to the lower portion of thecylindrical opening is believed to be relatively large. Therefore, TAT-DMAE employed as precursors in accordance with exemplary embodiments of the present invention can form a Ta2O.sub.5 layer exhibiting superior coverage to the conventional PET. Not intending to be bound by theory, it is believed that the discrepancies in vapor pressures can be attributed to a steric effect. According to Bradley, "Metal Alkoxides as Precursors for Electronic and Ceramic Materials" American ChemicalSociety, Chem. Rev., (1989), small alkoxides have a greater tendency to form oligomers such as dimers, trimers, etc. by bridging alkoxide groups than alkoxides having greater steric bulk. This discrepancy is believed to exert a sizeable influence onalkoxide vapor pressure. Accordingly, since an oxygen atom present in PET has a tendency to increase its coordination number by forming a covalent bond with a neighboring tantalum atom, the PET is likely to have the following molecular structure in a liquid state (seeFormula III). ##STR00003## Conversely, with respect to a TAT-DMAE embodiment, because a nitrogen atom, which has a covalent bond with oxygen, has a coordination bond with a Ta atom, the TAT-DMAE exists as a monomer in a liquid state and can be expressed by the followingstructural formula (see Formula IV). ##STR00004## Accordingly, it is believed that since PET has a higher thermal stability than the TAT-DMAE precursors utilized in the exemplary embodiments of the present invention, the PET requires more energy to break a bond between molecules to bevolatilized and thus has a lower vapor pressure. Another factor that potentially influences precursor coverage relates to sticking probability. According to Kawahara, "Conformal Step Coverage of (Ba, Sr)TiO3 Films Prepared by Liquid Source CVD Using Ti(t-BuO2)2(DPM)2",Japanese Journal of Applied Physics, Vol. 38, pp. 2205-2209, when Ti(t-BuO2)2(DPM)2 precursors are used, (Ba, Sr)TiO3 Films have superior step coverage relative to embodiments which employ Ti(DPM)2 precursors. Because thesticking probability of the Ti(t-BuO2)2(DPM)2 referenced by Kawahara is estimated to be about 0.02, and the sticking probability of the Ti(DPM)2 is estimated to be about 0.1, a thin film having superior coverage can be obtained whenthe sticking probability is low. According to Si-woo Lee et al., "Chemical Vapor Deposition Precursors for (Ba, Sr)TiO3 Films", 6th Korean Semiconductor Seminar, the deposition of Ti may be carried out using the surface reaction as a rate determining step, and highcoverage may be achieved by virtue of the surface movement of Ti. In view of all potential factors, and although not intending to be bound by any particular theory, it is believed that Ti precursors possessing low sticking probability are particularly suitable for forming thin films having a high degree ofcoverage, presumably due to relative ease of surface movement. With respect to precursor steric hindrance, since generally bulky precursors have a higher sticking probability than small precursors, the TAT-DMAE precursors may have a lower stickingprobability than that of PET, and thus, this may explain the superior step coverage of TAT-DMAE. FIG. 11 illustrates an adsorption mechanism of gaseous tantalum precursors on an Ru lower electrode according to an exemplary embodiment of the present invention. As reflected in FIG. 11, the mechanism in which the tantalum precursors reach thelower portion of the opening 240 formed by the Ru lower electrode 210 is believed to be attributable to: (a) surface movement 11 from the upper portion of the opening 240 or (b) direct transmission 12 to the lower portion of the opening 240. Accordingly, as shown in FIG. 9A or FIG. 10, in order to minimize or reduce oxidation of Ru in the lower portion of the Ru lower electrode 210, the provided tantalum precursors may be uniformly adsorbed and may cover the entire lower electrode 210 bysurface diffusion or direct transmission. In order to carry out this procedure in optimal fashion, surface movement of the precursors adsorbed on the substrate may be unencumbered, and the vapor pressure should be sufficiently high to accommodate a plurality of precursors. Inparticular, precursors such as TAT-DMAE according to exemplary embodiments of the present invention typically possess a higher vapor pressure and superior surface movement relative to conventional precursors such as PET, thereby forming a Ta2O.sub.5layer exhibiting improved coverage. Although the above exemplary embodiments illustrate HfO2 films and Ta2O.sub.5 film, it is apparent to any person skilled in the art to apply an ALD process according to the present invention to various metal oxides such as ZrO2,Nb2O.sub.5, Al2O.sub.3, TiO2, CeO2, In2O.sub.3 and RuO2 In the case of Al2O.sub.3, aluminum alkoxide precursors such as Al[OC2H.sub.5]3 or Al(OCH(CH3)2)3 and an activated oxidant such as O3, plasma O2, remote plasma O2 or plasma N2O may be used. ATiO2 film may be deposited by ALD process using titanium alkoxide precursors such as Ti[OC2H.sub.5]4 or Ti(OCH(CH3)2)4 and an activated oxidant. In the case of Nb2O.sub.5, a niobium alkoxide precursor such asNb[OC2H.sub.5]5 may be used. In the case of ZrO2, a zirconium alkoxide precursor such as Zr(OtBu)4 may be used. According to exemplary embodiments of the present invention as described above, a thin film is deposited by ALD process using one or more metal alkoxide precursors and one or more activated oxidants that contain no hydroxyl group. The thin filmmanufactured by exemplary embodiments of the present invention show improved dielectric characteristics including reduced leakage current and improved step coverage. Although the exemplary embodiments of the present invention have been described, it is understood that the present invention should not be limited to these exemplary embodiments but various changes and modifications can be made by one skilled inthe art within the spirit and scope of the present invention as hereinafter claimed. Field of SearchHAVING MAGNETIC OR FERROELECTRIC COMPONENTHaving high dielectric constant insulator (e.g., Ta2O5, etc.) Insulative material is compound of refractory group metal (i.e., titanium (Ti), zirconium (Zr), hafnium (Hf), vanadium (V), niobium (Nb), tantalum (Ta), chromium (Cr), molybdenum (Mo), tungsten (W), or alloy thereof) |
